Canonical Allele Identifier: CA2576369063
Gene: PRKAR1A HGNC NCBI
FAM20A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.68540791dup , CM000679.2:g.68540791dup GRCh38
NC_000017.10:g.66536932dup , CM000679.1:g.66536932dup GRCh37
NC_000017.9:g.64048527dup NCBI36
NG_007093.3:g.132169dup , LRG_514:g.132169dup
NG_029809.1:g.65167dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000588188.7:c.974-10293dup (PRKAR1A) ENSP00000468106.2:n.974-10293dup
ENST00000711037.1:c.974-10293dup (PRKAR1A) ENSP00000518555.1:n.974-10293dup
ENST00000585981.6:c.974-10293dup (PRKAR1A) ENSP00000467311.2:n.974-10293dup
ENST00000592554.2:c.1219+61dup (FAM20A) MANE Select ENSP00000468308.1:n.1219+61dup
ENST00000226094.9:n.897+61dup (FAM20A)
ENST00000375556.8:n.1143+61dup (FAM20A)
ENST00000588188.6:c.974-10293dup (PRKAR1A) ENSP00000468106.2:n.974-10293dup
ENST00000590074.5:c.1375+61dup (FAM20A)
ENST00000590873.5:c.42-822dup (FAM20A) ENSP00000467884.1:n.42-822dup
ENST00000592554.1:c.1219+61dup (FAM20A) ENSP00000468308.1:n.1219+61dup
NM_001243746.1:c.805+61dup (FAM20A) NP_001230675.1:n.805+61dup
NM_001276290.1:c.974-10293dup (PRKAR1A) NP_001263219.1:n.974-10293dup
NM_017565.3:c.1219+61dup (FAM20A) NP_060035.2:n.1219+61dup
NR_027751.1:n.934+61dup (FAM20A)
XM_006721959.2:c.805+61dup (FAM20A) XP_006722022.1:n.805+61dup
XM_011524917.1:c.1099+61dup (FAM20A) XP_011523219.1:n.1099+61dup
XR_934486.1:n.1347+61dup (FAM20A)
XR_934487.1:n.1347+61dup (FAM20A)
XR_934489.1:n.1256+61dup (FAM20A)
XR_934490.1:n.1256+61dup (FAM20A)
XM_006721959.3:c.805+61dup (FAM20A) XP_006722022.1:n.805+61dup
XR_001752544.2:n.1315+61dup (FAM20A)
XR_002958041.1:n.1290+61dup (FAM20A)
XR_934487.3:n.1290+61dup (FAM20A)
NM_017565.4:c.1219+61dup (FAM20A) MANE Select NP_060035.2:n.1219+61dup
NM_001243746.2:c.805+61dup (FAM20A) NP_001230675.1:n.805+61dup
NR_027751.2:n.934+61dup (FAM20A)